FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KSEA CALCUSPLIT

K Number: K992114 · Decision Aug 18, 1999
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
60
Applicant Total
35
Review Days
57

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Basic Information

Device Name
KSEA CALCUSPLIT
K Number
K992114
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4480
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Karl Storz Endoscopy
Date Received
June 22, 1999
Decision Date
August 18, 1999
Product Code
FFK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FFK Lithotriptor, Electro-Hydraulic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FFK), ordered by most recent decision date.

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Other Clearances by Karl Storz Endoscopy

K Number Device Name
K043375 FISCH TITANIUM MIDDLE EAR PROSTHESES
K030848 PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K030009 KSEA POWERSHAVER SYSTEM S2
K023924 AUTOCON II 200 ELECTROSURGICAL GENERATOR
K023187 KSEA SPINOSCOPE
K011700 MODULITH SLK LITHOTRIPTER
K021776 KSEA QUADRO SWITCH
K013107 BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K011841 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K010569 KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
Search all 35 clearances from Karl Storz Endoscopy →